上海交通大学学报(医学版)
上海交通大學學報(醫學版)
상해교통대학학보(의학판)
JOURNAL OF SHANGHAI JIAOTONG UNIVERSITY(MEDICAL SCIENCE)
2010年
4期
381-385
,共5页
赵丽娟%余娇%李影%陈奕%夏芳珍%王宁荐%陆颖理
趙麗娟%餘嬌%李影%陳奕%夏芳珍%王寧薦%陸穎理
조려연%여교%리영%진혁%하방진%왕저천%륙영리
大鼠品系%肝脏卵圆细胞%细胞增殖模型%细胞分选%细胞培养
大鼠品繫%肝髒卵圓細胞%細胞增殖模型%細胞分選%細胞培養
대서품계%간장란원세포%세포증식모형%세포분선%세포배양
rat strains%hepatic oval cells%animal proliferation model%cell sorting%cell culture
目的 对不同品系大鼠肝卵圆细胞增殖模型进行比较,筛选建模效率较高的大鼠品系.方法 选择F344、Wistar和SD大鼠各10只,经2-乙酰氨基芴灌胃和四氯化碳腹腔注射建立肝脏卵圆细胞增殖模型,组织学和免疫组织化学检测鉴定.荧光激活细胞筛选法分选并纯化各品系大鼠肝脏卵圆细胞,分析Thy-1.1~+细胞百分率,观察Thy-1.1~+细胞培养结果.结果 成功建立三种品系大鼠肝脏卵圆细胞增殖模型.流式细胞仪分选结果显示,F344、wistar和SD大鼠Thy-1.1~+细胞百分率分别为(9.46±0.99)%、(2.46±0.37)%和(1.46±0.12)%;各品系大鼠间Thy-1.1~+细胞百分率比较,差异有统计学意义(P<0.05).细胞培养观察发现,与Wistar和SD大鼠比较,F344大鼠分选得到的肝脏卵圆细胞生长状态好且纯度较高.结论 在用于建立肝脏卵圆细胞增殖模型最为常见的三种品系大鼠中,F344大鼠所建模型的肝脏卵圆细胞活化效率最高.
目的 對不同品繫大鼠肝卵圓細胞增殖模型進行比較,篩選建模效率較高的大鼠品繫.方法 選擇F344、Wistar和SD大鼠各10隻,經2-乙酰氨基芴灌胃和四氯化碳腹腔註射建立肝髒卵圓細胞增殖模型,組織學和免疫組織化學檢測鑒定.熒光激活細胞篩選法分選併純化各品繫大鼠肝髒卵圓細胞,分析Thy-1.1~+細胞百分率,觀察Thy-1.1~+細胞培養結果.結果 成功建立三種品繫大鼠肝髒卵圓細胞增殖模型.流式細胞儀分選結果顯示,F344、wistar和SD大鼠Thy-1.1~+細胞百分率分彆為(9.46±0.99)%、(2.46±0.37)%和(1.46±0.12)%;各品繫大鼠間Thy-1.1~+細胞百分率比較,差異有統計學意義(P<0.05).細胞培養觀察髮現,與Wistar和SD大鼠比較,F344大鼠分選得到的肝髒卵圓細胞生長狀態好且純度較高.結論 在用于建立肝髒卵圓細胞增殖模型最為常見的三種品繫大鼠中,F344大鼠所建模型的肝髒卵圓細胞活化效率最高.
목적 대불동품계대서간란원세포증식모형진행비교,사선건모효솔교고적대서품계.방법 선택F344、Wistar화SD대서각10지,경2-을선안기물관위화사록화탄복강주사건립간장란원세포증식모형,조직학화면역조직화학검측감정.형광격활세포사선법분선병순화각품계대서간장란원세포,분석Thy-1.1~+세포백분솔,관찰Thy-1.1~+세포배양결과.결과 성공건립삼충품계대서간장란원세포증식모형.류식세포의분선결과현시,F344、wistar화SD대서Thy-1.1~+세포백분솔분별위(9.46±0.99)%、(2.46±0.37)%화(1.46±0.12)%;각품계대서간Thy-1.1~+세포백분솔비교,차이유통계학의의(P<0.05).세포배양관찰발현,여Wistar화SD대서비교,F344대서분선득도적간장란원세포생장상태호차순도교고.결론 재용우건립간장란원세포증식모형최위상견적삼충품계대서중,F344대서소건모형적간장란원세포활화효솔최고.
Objective To select the rat strain relatively more suitable for model establishment by comparison of hepatic oval cell proliferation models from different rat strains. Methods Ten F344 rats, 10 Wistar rats and 10 SD rats were selected, hepatic oval cell proliferation models were established respectively by intragastric administration of 2-acetylaminofluorene and intraperitoneally injection of carbon tetrachloride, and were identified by histological examination and immunohistochemical examination. Fluorescence-activated cell sorting was employed to separate and purify the hepatic oval cells from different rat strains, percentages of Thy-1. 1~+ cells were analysed, and culture results of Thy-1. 1~+ cells were observed. Results Hepatic oval cell proliferation models from three rat strains were successfully established. Fluorescence-activated cell sorting revealed that the percentages of Thy-1. 1~+ cells in F344 rats, Wistar Rats and SD rats were (9. 46 ± 0. 99) % , (2. 46 ± 0. 37) % and (1.46 ±0. 12) % , respectively, and there were significant differences in percentages of Thy-1. 1~+ cells among different rat strains (P <0.05). Observation of cell culture indicated that compared with Wistar rats and SD rats, hepatic oval cells separated from F344 rats were in better growth state and higher purifity. Conclusion Among the three rat strains most commonly used for hepatic oval cell proliferation models, hepatic oval cells from F344 rats have the highest activation efficiency.